NM_198578.4(LRRK2):c.7537G>A (p.Val2513Met) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 21, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004518013.1
Allele description [Variation Report for NM_198578.4(LRRK2):c.7537G>A (p.Val2513Met)]
NM_198578.4(LRRK2):c.7537G>A (p.Val2513Met)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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JGI_CAAJ23281.fwd NIH_XGC_tropBrn2 Xenopus tropicalis cDNA clone IMAGE:7650712 5...
JGI_CAAJ23281.fwd NIH_XGC_tropBrn2 Xenopus tropicalis cDNA clone IMAGE:7650712 5', mRNA sequencegi|58366722|gnl|dbEST|27504310|gb|C 95.1|Nucleotide
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Homo sapiens cDNA FLJ13941 fis, clone Y79AA1000850
Homo sapiens cDNA FLJ13941 fis, clone Y79AA1000850gi|10436241|dbj|AK024003.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024